Diabetic Dead-in-Bed Syndrome: A Possible Link to a Cardiac Ion Channelopathy
Author(s) -
Jonathan R. Skinner,
Renate MarquisNicholson,
Alix Luangpraseuth,
Rick Cutfield,
Jackie Crawford,
Donald R. Love
Publication year - 2014
Publication title -
case reports in medicine
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.2
H-Index - 20
eISSN - 1687-9627
pISSN - 1687-9635
DOI - 10.1155/2014/647252
Subject(s) - brugada syndrome , medicine , sudden cardiac death , ventricular fibrillation , sudden death , missense mutation , cardiology , diabetes mellitus , long qt syndrome , autopsy , hyperinsulinism , population , insulin , endocrinology , qt interval , insulin resistance , mutation , gene , genetics , environmental health , biology
Sudden unexpected nocturnal death among patients with diabetes occurs approximately ten times more commonly than in the general population. Malignant ventricular arrhythmia due to Brugada syndrome has been postulated as a cause, since a glucose-insulin bolus can unmask the Brugada electrocardiographic signature in genetically predisposed individuals. In this report we present a 16-year-old male with insulin-dependent diabetes who died suddenly at night. His diabetes had been well controlled, without significant hypoglycaemia. At autopsy, he had a full stomach and a glucose level of 7 mmol/L in vitreous humor, excluding hypoglycaemia. Genetic analysis of autopsy DNA revealed a missense mutation, c.370A>G (p.Ile124Val), in the GPD1L gene. A parent carried the same mutation and has QT prolongation. Mutations in this gene have been linked to Brugada syndrome and sudden infant death. The patient may have died from a ventricular arrhythmia, secondary to occult Brugada syndrome, triggered by a full stomach and insulin. The data suggest that molecular autopsies are warranted to investigate other cases of the diabetic dead-in-bed syndrome.
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